Planta

, Volume 220, Issue 2, pp 278–285 | Cite as

Salt stress enhances xylem development and expression of S-adenosyl-l-methionine synthase in lignifying tissues of tomato plants

  • Inmaculada Sánchez-Aguayo
  • José Manuel Rodríguez-Galán
  • Remedios García
  • José Torreblanca
  • José Manuel Pardo
Original Article

Abstract

S-Adenosyl-l-methionine synthase (SAM; ATP:l-methionine adenosyltransferase, EC 2.5.1.6) catalyzes the biosynthesis of S-adenosyl-l-methionine (AdoMet), a universal methyl-group donor. This enzyme is induced by salinity stress in tomato (Lycopersicon esculentum Mill.). To elucidate the role of SAM and AdoMet in the adaptation of plants to a saline environment, the expression pattern and histological distribution of SAM was investigated in control and salt-stressed tomato plants. Immunohistochemical analysis showed that SAM proteins were expressed in all cell types and plant organs, albeit with preferential accumulation in lignified tissues. Lignin deposition was estimated by histochemical tests and the extent of tissue lignification in response to salinity was quantified by image analysis. The average number of lignified cells in vascular bundles was significantly greater in plants under salt stress, with a maximal expansion of the lignified area found in the root vasculature. Accordingly, the greatest abundance of SAM gene transcripts and proteins occurred in roots. These results indicate that increased SAM activity correlated with a greater deposition of lignin in the vascular tissues of plants under salinity stress. A model is proposed in which an increased number of lignified tracheary elements in tomato roots under salt stress may enhance the cell-to-cell pathway for water transport, which would impart greater selectivity and reduced ion uptake, and compensate for diminished bulk flow of water and solutes along the apoplastic pathway.

Keywords

S-Adenosyl-l-methionine synthase Lignification Lycopersicon Salt stress Xylem 

Abbreviations

AdoMet

S-Adenosyl-l-methionine

SAM

S-Adenosyl-l-methionine synthase

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Copyright information

© Springer-Verlag 2004

Authors and Affiliations

  • Inmaculada Sánchez-Aguayo
    • 2
  • José Manuel Rodríguez-Galán
    • 1
  • Remedios García
    • 2
  • José Torreblanca
    • 2
  • José Manuel Pardo
    • 1
  1. 1.Instituto de Recursos Naturales y AgrobiologíaSevillaSpain
  2. 2.Departamento de Biología Celular, Facultad de BiologíaUniversidad de SevillaSevillaSpain

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